Instruction manual

6. Troubleshooting
6-4
RF-20A/20Axs
1 For details on the method for checking for air bubbles and contamination inside the cell, see:
^ "8.2 Inspection and Simple Washing of the Cell" P.8-5
Chromatogram
peaks are
trapezoidal.
The setting for [SENS] in the
parameter settings group is too
high.
Lower the setting for [SENS] in the
parameter settings group.
P.5-19
The concentration of the sample
is too high, or the volume poured
in is too large.
Dilute the sample or reduce the
volume poured in.
Spiking
Sawtooth
baseline
Continuous
spiking
Are air bubbles entrained in the
cell? (1)
Connect a back pressure device or
φ 0.3 mm × 2 m tubing to the flow
cell outlet tube and apply pressure.
Degas the mobile phase.
(Use the degasser.)
Continuous
spiking
Spiking that
occurs with
every pump
stroke
Have air bubbles built up inside
the cell? (1)
Connect a back pressure device or
φ 0.3 mm × 2 m tubing to the flow
cell outlet tube and apply pressure.
Using the syringe provided as an
accessory, clean the inside of the
flow cell with 2-propanol.
P. 8 - 5
Drift
Noise (large)
Rise
Is the cell contaminated? (1)
Disassemble the flow cell unit and
clean the cell. If the contamination
cannot be removed, replace the cell.
P. 8 -11
Is the lens soiled?
Disassemble the flow cell unit and
clean the lens. If the contamination
cannot be removed, replace the
lens.
If the drift stops when pumping is
stopped, have impurities become
entrained in the mobile phase?
Inspect the mobile phase and the
mobile phase flow line, and remove
impurities.
Wander of the
baseline
Is a strong airflow blowing directly
onto the instrument?
Prevent the airflow from blowing
directly onto the instrument by using
e.g. a screen.
Change the installation position.
Noise
corresponding
to the pump
stroke
Is the mobile phase pulsating?
Eliminate the pulsation from the
pump unit.
Use a pulsation absorption device.
Noise (large)
Deterioration or life expiry of the
lamp
Replace the lamp.
P.8-30
Symptom Probable Cause Corrective Action Page